Does SOLOSTAR Cause Incorrect product storage? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Incorrect product storage have been filed in association with SOLOSTAR. This represents 6.8% of all adverse event reports for SOLOSTAR.
51
Reports of Incorrect product storage with SOLOSTAR
6.8%
of all SOLOSTAR reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From SOLOSTAR?
Of the 51 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOLOSTAR. However, 51 reports have been filed with the FAERS database.
What Other Side Effects Does SOLOSTAR Cause?
Blood glucose increased (253)
Injection site pain (99)
Injection site haemorrhage (69)
Drug dose omission (59)
Visual impairment (57)
Blood glucose decreased (52)
Injection site bruising (52)
Injury associated with device (51)
Feeling abnormal (33)
Malaise (31)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which SOLOSTAR Alternatives Have Lower Incorrect product storage Risk?
SOLOSTAR vs SOLRIAMFETOL
SOLOSTAR vs SOLU-MEDROL
SOLOSTAR vs SOMATREM
SOLOSTAR vs SOMATROPIN
SOLOSTAR vs SONIDEGIB